Gconvert the haworth projection for a monosaccharide to its corresponding fischer projection. this molecule is a haworth projection of a six membered ring with one oxygen atom and five carbon atoms. carbons 1 and 2 have a hydroxy substituent pointing down. carbons 3 and 4 have a hydroxy substituent pointing up. carbon 6 has a c h 2 o h substituent pointing up. select the fischer projection that is the open chain version of the haworth projection. a fischer projection with a six carbon backbone. carbon one is an aldehyde and carbon six is part of the group c h 2 o h. carbons two and three have an hydroxide group on the right and carbons four and five have an hydroxide group on the left. a fischer projection with a six carbon backbone. carbon one is an aldehyde and carbon six is part of the group c h 2 o h. carbons two and five have an hydroxide group on the left and carbons three and four have an hydroxide group on the right. a fischer projection with a six carbon backbone. carbon one is an aldehyde and carbon six is part of the group c h 2 o h. carbons two and five have an hydroxide group on the right and carbons three and four have an hydroxide group on the left. a fischer projection with a six carbon backbone. carbon one is an aldehyde and carbon six is part of the group c h 2 o h. carbons two and three have an hydroxide group on the left and carbons four and five have an hydroxide group on the right.